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Generation of High-Amylose Rice through CRISPR/Cas9-Mediated Targeted Mutagenesis of Starch Branching Enzymes
Cereals high in amylose content (AC) and resistant starch (RS) offer potential health benefits. Previous studies using chemical mutagenesis or RNA interference have demonstrated that starch branching enzyme (SBE) plays a major role in determining the fine structure and physical properties of starch....
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339335/ https://www.ncbi.nlm.nih.gov/pubmed/28326091 http://dx.doi.org/10.3389/fpls.2017.00298 |
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author | Sun, Yongwei Jiao, Guiai Liu, Zupei Zhang, Xin Li, Jingying Guo, Xiuping Du, Wenming Du, Jinlu Francis, Frédéric Zhao, Yunde Xia, Lanqin |
author_facet | Sun, Yongwei Jiao, Guiai Liu, Zupei Zhang, Xin Li, Jingying Guo, Xiuping Du, Wenming Du, Jinlu Francis, Frédéric Zhao, Yunde Xia, Lanqin |
author_sort | Sun, Yongwei |
collection | PubMed |
description | Cereals high in amylose content (AC) and resistant starch (RS) offer potential health benefits. Previous studies using chemical mutagenesis or RNA interference have demonstrated that starch branching enzyme (SBE) plays a major role in determining the fine structure and physical properties of starch. However, it remains a challenge to control starch branching in commercial lines. Here, we use CRISPR/Cas9 technology to generate targeted mutagenesis in SBEI and SBEIIb in rice. The frequencies of obtained homozygous or bi-allelic mutant lines with indels in SBEI and SBEIIb in T(0) generation were from 26.7 to 40%. Mutations in the homozygous T(0) lines stably transmitted to the T(1) generation and those in the bi-allelic lines segregated in a Mendelian fashion. Transgene-free plants carrying only the frame-shifted mutagenesis were recovered in T(1) generation following segregation. Whereas no obvious differences were observed between the sbeI mutants and wild type, sbeII mutants showed higher proportion of long chains presented in debranched amylopectin, significantly increased AC and RS content to as higher as 25.0 and 9.8%, respectively, and thus altered fine structure and nutritional properties of starch. Taken together, our results demonstrated for the first time the feasibility to create high-amylose rice through CRISPR/Cas9-mediated editing of SBEIIb. |
format | Online Article Text |
id | pubmed-5339335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53393352017-03-21 Generation of High-Amylose Rice through CRISPR/Cas9-Mediated Targeted Mutagenesis of Starch Branching Enzymes Sun, Yongwei Jiao, Guiai Liu, Zupei Zhang, Xin Li, Jingying Guo, Xiuping Du, Wenming Du, Jinlu Francis, Frédéric Zhao, Yunde Xia, Lanqin Front Plant Sci Plant Science Cereals high in amylose content (AC) and resistant starch (RS) offer potential health benefits. Previous studies using chemical mutagenesis or RNA interference have demonstrated that starch branching enzyme (SBE) plays a major role in determining the fine structure and physical properties of starch. However, it remains a challenge to control starch branching in commercial lines. Here, we use CRISPR/Cas9 technology to generate targeted mutagenesis in SBEI and SBEIIb in rice. The frequencies of obtained homozygous or bi-allelic mutant lines with indels in SBEI and SBEIIb in T(0) generation were from 26.7 to 40%. Mutations in the homozygous T(0) lines stably transmitted to the T(1) generation and those in the bi-allelic lines segregated in a Mendelian fashion. Transgene-free plants carrying only the frame-shifted mutagenesis were recovered in T(1) generation following segregation. Whereas no obvious differences were observed between the sbeI mutants and wild type, sbeII mutants showed higher proportion of long chains presented in debranched amylopectin, significantly increased AC and RS content to as higher as 25.0 and 9.8%, respectively, and thus altered fine structure and nutritional properties of starch. Taken together, our results demonstrated for the first time the feasibility to create high-amylose rice through CRISPR/Cas9-mediated editing of SBEIIb. Frontiers Media S.A. 2017-03-07 /pmc/articles/PMC5339335/ /pubmed/28326091 http://dx.doi.org/10.3389/fpls.2017.00298 Text en Copyright © 2017 Sun, Jiao, Liu, Zhang, Li, Guo, Du, Du, Francis, Zhao and Xia. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Sun, Yongwei Jiao, Guiai Liu, Zupei Zhang, Xin Li, Jingying Guo, Xiuping Du, Wenming Du, Jinlu Francis, Frédéric Zhao, Yunde Xia, Lanqin Generation of High-Amylose Rice through CRISPR/Cas9-Mediated Targeted Mutagenesis of Starch Branching Enzymes |
title | Generation of High-Amylose Rice through CRISPR/Cas9-Mediated Targeted Mutagenesis of Starch Branching Enzymes |
title_full | Generation of High-Amylose Rice through CRISPR/Cas9-Mediated Targeted Mutagenesis of Starch Branching Enzymes |
title_fullStr | Generation of High-Amylose Rice through CRISPR/Cas9-Mediated Targeted Mutagenesis of Starch Branching Enzymes |
title_full_unstemmed | Generation of High-Amylose Rice through CRISPR/Cas9-Mediated Targeted Mutagenesis of Starch Branching Enzymes |
title_short | Generation of High-Amylose Rice through CRISPR/Cas9-Mediated Targeted Mutagenesis of Starch Branching Enzymes |
title_sort | generation of high-amylose rice through crispr/cas9-mediated targeted mutagenesis of starch branching enzymes |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339335/ https://www.ncbi.nlm.nih.gov/pubmed/28326091 http://dx.doi.org/10.3389/fpls.2017.00298 |
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